ValueSet-2.16.840.1.113883.17.4077.2.1007

Sourceus.nlm.vsac#0.11.0:null (v4.0.1)
resourceTypeValueSet
id2.16.840.1.113883.17.4077.2.1007
canonicalhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.17.4077.2.1007
version20200909
statusactive
publisherACEP/AMA-PCPI Steward
nameCoagulopathiesExcludingThrombocytopenia
titleCoagulopathies Excluding Thrombocytopenia
date2020-09-09T01:00:54-04:00
experimentalfalse
Usages

This value set contains 18 concepts

Code System Display
   D65 http://hl7.org/fhir/sid/icd-10-cm Disseminated intravascular coagulation [defibrination syndrome]
   D66 http://hl7.org/fhir/sid/icd-10-cm Hereditary factor VIII deficiency
   D67 http://hl7.org/fhir/sid/icd-10-cm Hereditary factor IX deficiency
   D68.0 http://hl7.org/fhir/sid/icd-10-cm Von Willebrand disease
   D68.1 http://hl7.org/fhir/sid/icd-10-cm Hereditary factor XI deficiency
   D68.2 http://hl7.org/fhir/sid/icd-10-cm Hereditary deficiency of other clotting factors
   D68.311 http://hl7.org/fhir/sid/icd-10-cm Acquired hemophilia
   D68.312 http://hl7.org/fhir/sid/icd-10-cm Antiphospholipid antibody with hemorrhagic disorder
   D68.318 http://hl7.org/fhir/sid/icd-10-cm Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
   D68.32 http://hl7.org/fhir/sid/icd-10-cm Hemorrhagic disorder due to extrinsic circulating anticoagulants
   D68.4 http://hl7.org/fhir/sid/icd-10-cm Acquired coagulation factor deficiency
   D68.8 http://hl7.org/fhir/sid/icd-10-cm Other specified coagulation defects
   D68.9 http://hl7.org/fhir/sid/icd-10-cm Coagulation defect, unspecified
   D69.1 http://hl7.org/fhir/sid/icd-10-cm Qualitative platelet defects
   D69.41 http://hl7.org/fhir/sid/icd-10-cm Evans syndrome
   D69.51 http://hl7.org/fhir/sid/icd-10-cm Posttransfusion purpura
   D69.8 http://hl7.org/fhir/sid/icd-10-cm Other specified hemorrhagic conditions
   D69.9 http://hl7.org/fhir/sid/icd-10-cm Hemorrhagic condition, unspecified

Produced 08 Sep 2023